NCT07059624Recruiting
Femoral Arterial Cannulation in Pediatrics
Femoral Arterial Cannulation Performed by Anesthesia Residents: A Comparison Between Ultrasound-Guided "Modified Dynamic Needle Tip Positioning, Short-Axis, Out-Of-Plane" and "Conventional, Short-Axis, Out-Of-Plane" Methods
Source: ClinicalTrials.gov · Last updated 20 Jul 2025 · Not updated for over 12 months - ask the site whether it is still open
Brief summary (registry, in English)
The goal of this clinical trial\] is to evaluate the efficacy and safety of the ultrasound-guided "Modified Dynamic Needle Tip Positioning Short-Axis, Out-Of-Plane" (MDNTP-SAOP) technique compared to the "Conventional, Short-Axis, Out-Of-Plane" (C-SAOP) technique for femoral arterial cannulation performed by anesthesia residents in children. The main question it aims to answer is: What is the time required for attempted femoral arterial cannulation by anesthesia residents at the first puncture site? Researchers will compare the efficacy and safety of MDNTP-SAOP versus C-SAOP methods for femoral arterial cannulation performed by anesthesia residents in infants and children undergoing cardiac surgery. Participants will be randomized to either the MDNTP-SAOP or the C-SAOP group. Intraoperatively, time taken for attempted cannulation by the resident at the first site of femoral arterial puncture, number of attempts at arterial cannulation, and number of cannulae required for successful cannula insertion will be recorded. Adverse events will be monitored on postoperative days 1 and 3. The insertion site will be examined for thrombosis, hematoma, infection, or limb ischemia distal to the insertion site
- Status (registry)
- Recruiting
- Study type
- Interventional
- Enrollment
- 80 (estimated)
- First submitted
- 8 Jul 2025
- Start date
- 9 Jul 2025
- Primary completion date
- 1 Jan 2027
- Lead sponsor
- American University of Beirut Medical Center
- NCT number
- NCT07059624
What you commit to
- Study type: Interventional
- Planned participants: 80
- From 9 Jul 2025 to the primary completion date, 1 Jan 2027
- 1 site in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Need for emergency surgery.
Other
- Hemodynamic instability.
Who the study is looking for
- Infants and children under 12 years of age.
- American Society of Anesthesiologist (ASA) physical status II-IV.
- Patients with congenital heart disease undergoing cardiac surgery who do not have existing arterial line access.
Age in the registry: - to 12 years · Sex: All · Accepts healthy volunteers
Sites (1)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| American University of Beirut Medical Center Coordinator of this site? Confirm its status | Beirut | Lebanon | Recruiting |
This page is information, not medical advice. Discuss any trial with your doctor.